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Impurity reference standards

Dipyridamole impurity standards

This page brings together 12 Dipyridamole related compounds that analytical teams use to identify, quantify and control impurities in the active ingredient and the finished dosage form. The range includes 7 pharmacopoeial impurities and 1 isotope-labelled standard.

12reference materials
7pharmacopoeial
1isotope labelled
Dipyridamole structure
Parent API

Dipyridamole

CAS
58-32-2
Formula
C24H40N8O4
MW
504.6 g/mol
Code
ZX-006505

Each lot ships with a certificate of analysis, and characterisation data such as 1H-NMR, mass spectrum and HPLC purity can be shared before you order. Typical uses are method development and validation, relative response factor work, forced degradation studies and the impurity sections of ANDA, DMF or CEP filings.

By impurity type

Pharmacopoeial7EP, USP, BP or JP named impurities
Isotope labelled1Deuterated, 13C or 15N internal standards

Counts are based on product names. One compound can fall into more than one type.

All Dipyridamole reference materials

1–12 of 12 standards
Questions

Dipyridamole impurities, answered

What Dipyridamole reference materials are available?
The catalogue currently lists 12 compounds for Dipyridamole, including 7 pharmacopoeial impurities and 1 isotope-labelled standard. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Dipyridamole impurity standard?
A certificate of analysis travels with every lot. On request we share the characterisation set, usually 1H-NMR, mass spectrum, HPLC purity and IR, and for some materials TGA or water content. Ask for the data before ordering if your QA team needs to review it.
Can Zemixal make a Dipyridamole impurity that is not listed?
Often yes. Send the structure, name or CAS number with the quantity you need and our sourcing team checks custom synthesis options, usually from 10 mg up to gram scale, with a quoted lead time.
Are isotope-labelled Dipyridamole standards available?
Yes. 1 stable-isotope labelled compound is listed, suitable as internal standards for LC-MS bioanalysis and trace impurity quantitation.
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